Human NK cell education by inhibitory receptors for MHC class I

被引:988
作者
Anfossi, Nicolas
Andre, Pascale
Guia, Sophie
Falk, Christine S.
Roetynck, Sophie
Stewart, C. Andrew
Breso, Violette
Frassati, Coralie
Reviron, Denis
Middleton, Derek
Romagne, Francois
Ugolini, Sophie [1 ]
Vivier, Eric
机构
[1] Univ Mediterranee, Dtr Immunol marseille Luminy, F-13009 Marseille, France
[2] Innate Pharma, F-13009 Marseille, France
[3] INSERM, U631, F-13009 Marseille, France
[4] CNRS, UMR6102, F-13009 Marseille, France
[5] Natl Res Ctr Environm & Hlth, Inst Mol Immunol, D-81377 Munich, Germany
[6] Etab Francais Sang Alpes Mediterranee, F-13392 Marseille, France
[7] City Hosp, No Ireland Histocompatibil & Immunogenet Lab, Belfast BT9 7TS, Antrim, North Ireland
[8] Hop Marseille, Hop Concept Assistance Publ, F-13385 Marseille, France
关键词
D O I
10.1016/j.immuni.2006.06.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Natural killer (NK) cells recognize the absence of self MHC class I as a way to discriminate normal cells from cells in distress. In humans, this "missing self" recognition is ensured by inhibitory receptors such as KIR, which dampen NK cell activation upon interaction with their MHC class I ligands. We show here that NK cells lacking inhibitory KIR for self MHC class I molecules are present in human peripheral blood. These cells harbor a mature NK cell phenotype but are hyporesponsive to various stimuli, including MHC class I-deficient target cells. This response is in contrast to NK cells that express a single inhibitory KIR specific for self MHC class 1, which are functionally competent when exposed to the same stimuli. These results show the involvement of KIR-MHC class I interactions in the calibration of NK cell effector capacities, suggesting its role in the subsequent "missing self" recognition.
引用
收藏
页码:331 / 342
页数:12
相关论文
共 41 条
[1]
Modification of P-selectin glycoprotein ligand-1 with a natural killer cell-restricted sulfated lactosamine creates an alternate ligand for L-selectin [J].
André, P ;
Spertini, O ;
Guia, S ;
Rihet, P ;
Dignat-George, F ;
Brailly, H ;
Sampol, J ;
Anderson, PJ ;
Vivier, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3400-3405
[2]
DAP12-deficient mice fail to develop autoimmunity due to impaired antigen priming [J].
Bakker, ABH ;
Hoek, RM ;
Cerwenka, A ;
Blom, B ;
Lucian, L ;
McNeil, T ;
Murray, R ;
Phillips, JH ;
Sedgwick, JD ;
Lanier, LL .
IMMUNITY, 2000, 13 (03) :345-353
[3]
A structural perspective on MHC class I recognition by killer cell immunoglobulin-like receptors [J].
Boyington, JC ;
Sun, PD .
MOLECULAR IMMUNOLOGY, 2002, 38 (14) :1007-1021
[4]
Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells [J].
Bryceson, YT ;
March, ME ;
Barber, DF ;
Ljunggren, HG ;
Long, EO .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (07) :1001-1012
[5]
Carrington M, 2006, CURR TOP MICROBIOL, V298, P225
[6]
Cooper GJS, 2001, AUST J DAIRY TECHNOL, V56, P97
[7]
Development of a PCR-SSOP approach capable of defining the natural killer cell inhibitory receptor (KIR) gene sequence repertoires [J].
Crum, KA ;
Logue, SE ;
Curran, MD ;
Middleton, D .
TISSUE ANTIGENS, 2000, 56 (04) :313-326
[8]
Daëron M, 1999, CURR TOP MICROBIOL, V244, P1
[9]
Major histocompatibility complex genes determine natural killer cell tolerance [J].
Dorfman, JR ;
Raulet, DH .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (01) :151-155
[10]
NK cell compartments and their activation by dendritic cells [J].
Ferlazzo, G ;
Münz, C .
JOURNAL OF IMMUNOLOGY, 2004, 172 (03) :1333-1339